Monomolecular triplet decay dynamics in fluorene-based conjugated polymer films studied by transient absorption spectroscopy

被引:15
作者
Ohkita, H.
Cook, S.
Ford, T. A.
Greenham, N. C.
Durrant, J. R.
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Chem, London SW7 2AZ, England
[2] Univ Cambridge, Cavendish Lab, Cambridge CB3 0HE, England
基金
英国工程与自然科学研究理事会; 日本学术振兴会;
关键词
fluorene polymers; triplet state; intersystem crossing; temperature dependence; transient absorption spectroscopy;
D O I
10.1016/j.jphotochem.2006.04.026
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Monomolecular decay dynamics of triplet excited states formed in fluorene-based conjugated polymer pristine and blend films were studied by transient absorption spectroscopy over the temperature range 77-300 K. The decay rate was temperature independent below 150 K and steeply increased above 150 K. The temperature dependence from 150 to 300 K was expressed by the Arrhenius equation with an activation energy of 0.12 eV. The thermal activation process was assigned to the temperature-dependent non-radiative decay of triplet excitons, which might result from the spin-orbit coupling enhanced by vibrational motions in F8BT. The same tendency was observed for blend films, although with slightly faster decay dynamics, suggesting that the thermal activation process reflects an intrinsic photophysical property of the fluorene-based polymer. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:225 / 230
页数:6
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